HGVS | Genome Assembly |
---|---|
NC_000008.11:g.142914367T>G , CM000670.2:g.142914367T>G | GRCh38 |
NC_000008.10:g.143995783T>G , CM000670.1:g.143995783T>G | GRCh37 |
NC_000008.9:g.143992785T>G | NCBI36 |
NG_008374.1:g.8477A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323110.2:c.851A>C (CYP11B2) MANE Select | ENSP00000325822.2:p.Gln284Pro | |
ENST00000522728.5:c.264+322T>G (GML) | ENSP00000430799.1:n.264+322T>G | |
NM_000498.3:c.851A>C (CYP11B2) MANE Select | NP_000489.3:p.Gln284Pro | |
XM_011516877.1:c.929A>C (CYP11B2) | XP_011515179.1:p.Gln310Pro | |
XM_011516878.1:c.929A>C (CYP11B2) | XP_011515180.1:p.Gln310Pro | |
XM_011516879.1:c.851A>C (CYP11B2) | XP_011515181.1:p.Gln284Pro | |
XM_011516970.1:c.297+322T>G (GML) | XP_011515272.1:n.297+322T>G |